Hemophilia C is an autosomal inherited form of the disease. It affects biological males and females equally because the genetic defect that causes this type of hemophilia isn’t related to sex ...

This spontaneous mutation pattern explains why hemophilia A can appear unexpectedly in families with no known bleeding disorders. Genetic testing now allows precise identification of the specific ...

Researchers from the Centenary Institute have uncovered a reason why some people with hemophilia A develop resistance to ...

For centuries, hemophilia was a dangerous genetic disorder with no treatment. Children with hemophilia often didn't make it to adulthood, since a bump or fall could cause massive internal bleeding.

Genentech’s short film draws on the experiences of multiple families caring for children with hemophilia A, seeking to ...

A man’s acquired hemophilia coincided with a rare liver disease, a connection that had not been reported before, per a case ...

FVIII, the blood clotting protein missing in hemophilia A, adopts multiple shapes, making it more likely to be targeted by ...

Hemophilia is a genetic bleeding disorder that affects the body's ability to form blood clots, leading to prolonged bleeding, joint and muscle damage, disability, and, in severe cases, life ...

There is a need to raise awareness among the public about genetic disorders such as thalassemia, sickle cell anemia and hemophilia, all of which require continuous medication, said Minister for ...